<p>Capnometry measures end-tidal carbon dioxide (P<sub>Et</sub>CO<sub>2</sub>) in expired air and is standard practice for monitoring mechanical ventilation in pediatric critical care. P<sub>Et</sub>CO<sub>2</sub> is often used as a non-invasive indicator for arterial CO<sub>2</sub> (P<sub>a</sub>CO<sub>2</sub>), while under normal conditions the P<sub>a</sub>CO<sub>2</sub>-P<sub>Et</sub>CO<sub>2</sub> difference is 2–5 mmHg due to imperfect matching of ventilation-perfusion (V/Q). However, in some pediatric patients, a reversed (negative) P(a-Et)CO<sub>2</sub> gradient (ventilatory gap) can be observed, where P<sub>Et</sub>CO<sub>2</sub> exceeds P<sub>a</sub>CO<sub>2</sub>. While this phenomenon is commonly linked to underlying technicalities, physiological explanations, including relatively high closing volumes in infants, poorly compliant lung tissue, and elevated mixed venous CO₂ (Pv̅CO₂) due to increased CO₂ production during critical illness, have also been described in the literature. However, current evidence for these mechanisms is limited, and further research is needed to clarify their roles. Possibly, awareness of both technical and physiological factors that may underlie a negative P(a–Et)CO₂ gradient can help clinicians interpret observations more cautiously and consider appropriate adjustments to mechanical ventilation strategies as needed.</p>

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Reversed ventilatory gap capnometry in ventilated pediatric patients: a brief review for evidence of technical and physiological mechanisms

  • R. Klein-Blommert,
  • Reinout A. Bem,
  • D. G. Markhorst

摘要

Capnometry measures end-tidal carbon dioxide (PEtCO2) in expired air and is standard practice for monitoring mechanical ventilation in pediatric critical care. PEtCO2 is often used as a non-invasive indicator for arterial CO2 (PaCO2), while under normal conditions the PaCO2-PEtCO2 difference is 2–5 mmHg due to imperfect matching of ventilation-perfusion (V/Q). However, in some pediatric patients, a reversed (negative) P(a-Et)CO2 gradient (ventilatory gap) can be observed, where PEtCO2 exceeds PaCO2. While this phenomenon is commonly linked to underlying technicalities, physiological explanations, including relatively high closing volumes in infants, poorly compliant lung tissue, and elevated mixed venous CO₂ (Pv̅CO₂) due to increased CO₂ production during critical illness, have also been described in the literature. However, current evidence for these mechanisms is limited, and further research is needed to clarify their roles. Possibly, awareness of both technical and physiological factors that may underlie a negative P(a–Et)CO₂ gradient can help clinicians interpret observations more cautiously and consider appropriate adjustments to mechanical ventilation strategies as needed.